EP1209152A4 - Derives d'acide omega-amino-alpha-hydroxycarboxylique possedant un antagonisme alpha v beta 3 d'integrine - Google Patents
Derives d'acide omega-amino-alpha-hydroxycarboxylique possedant un antagonisme alpha v beta 3 d'integrineInfo
- Publication number
- EP1209152A4 EP1209152A4 EP00949959A EP00949959A EP1209152A4 EP 1209152 A4 EP1209152 A4 EP 1209152A4 EP 00949959 A EP00949959 A EP 00949959A EP 00949959 A EP00949959 A EP 00949959A EP 1209152 A4 EP1209152 A4 EP 1209152A4
- Authority
- EP
- European Patent Office
- Prior art keywords
- alpha
- antagonism
- omega
- beta
- amino
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
L'invention porte sur des composés de la formule générale (I) qui sont extrêmement solubles dans l'eau et qui possèdent un antagonisme αvβ3 d'intégrine. Dans cette formule, A représente un groupe hétérocyclique constitué de 5 à 7 éléments, éventuellement substitué, contenant 2 atomes d'hydrogène qui peuvent être fusionnés à d'autre noyaux ou -C(-NR?2) (=NR3¿); D représente une liaison, -NR4-, -O- ou -S- ; X et Z représentent chacun CH ou N; R7 et R8 représentent chacun alkyle C¿1-6?, halogéno, oxygène, etc.; Q représente > C=O, > CHR?13¿ ou > CHOR13 ; J représente une liaison ou alkylène C¿1-3?; R?1 à R4, R9 à R11 et R13¿ représentent chacun hydrogène, alkyle, etc.; m est un nombre entier compris entre 0 et 5 ; n est un nombre entier compris entre 0 et 4; et p et q sont chacun un nombre entier compris entre 1 et 3.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22209899 | 1999-08-05 | ||
JP22209899 | 1999-08-05 | ||
PCT/JP2000/005177 WO2001010844A1 (fr) | 1999-08-05 | 2000-08-02 | DERIVES D'ACIDE φ-AMINO-α-HYDROXYCARBOXYLIQUE POSSEDANT UN ANTAGONISME αvβ3 D'INTEGRINE |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1209152A1 EP1209152A1 (fr) | 2002-05-29 |
EP1209152A4 true EP1209152A4 (fr) | 2003-03-12 |
Family
ID=16777114
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP00949959A Withdrawn EP1209152A4 (fr) | 1999-08-05 | 2000-08-02 | Derives d'acide omega-amino-alpha-hydroxycarboxylique possedant un antagonisme alpha v beta 3 d'integrine |
Country Status (4)
Country | Link |
---|---|
US (1) | US6750219B1 (fr) |
EP (1) | EP1209152A4 (fr) |
AU (1) | AU6316900A (fr) |
WO (1) | WO2001010844A1 (fr) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8093246B2 (en) * | 2006-12-14 | 2012-01-10 | Lexicon Pharmaceuticals, Inc. | O-linked pyrimidin-4-amine-based compounds, compositions comprising them, and methods of their use to treat cancer |
Family Cites Families (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU642753B2 (en) | 1990-07-24 | 1993-10-28 | Mitsubishi Petrochemical Company Limited | Halogen-containing compounds, herbicidal composition containing the same as an active ingredient, and intermediary compounds therefor |
JPH0597818A (ja) | 1991-10-01 | 1993-04-20 | Mitsubishi Petrochem Co Ltd | 新規なピリミジン誘導体およびそれを有効成分とする除草剤 |
WO1994021599A1 (fr) | 1993-03-17 | 1994-09-29 | Meiji Seika Kabushiki Kaisha | Nouveau compose a activite inhibitrice de l'agregation des plaquettes |
JPH10501222A (ja) | 1994-05-27 | 1998-02-03 | メルク エンド カンパニー インコーポレーテッド | 破骨細胞仲介骨吸収を抑制するための化合物 |
IL118325A0 (en) | 1995-05-25 | 1996-10-31 | Pont Merck And Pharmaceutical | Integrin receptor antagonists and pharmaceutical compositions containing them |
EP0910563B1 (fr) | 1995-06-29 | 2003-05-02 | Smithkline Beecham Corporation | Antagonistes du recepteur de l'integrine |
CA2230209A1 (fr) | 1995-08-30 | 1997-03-06 | G.D. Searle & Co. | Derives de la meta-guanidine, de l'uree, de la thio-uree ou de l'acide aminobenzoique azacyclique utilises comme antagonistes de l'integrine |
AU1345697A (en) | 1995-12-22 | 1997-07-17 | Du Pont Merck Pharmaceutical Company, The | Novel integrin receptor antagonists |
DE19548709A1 (de) | 1995-12-23 | 1997-07-03 | Merck Patent Gmbh | Tyrosinderivate |
JP2000502354A (ja) | 1995-12-29 | 2000-02-29 | スミスクライン・ビーチャム・コーポレイション | ビトロネクチン受容体アンタゴニスト |
ZA9610853B (en) | 1995-12-29 | 1998-04-06 | Smithkline Beecham Corp | Processes and intermediates for preparing pharmaceuticals. |
JP2000516197A (ja) | 1996-01-16 | 2000-12-05 | メルク エンド カンパニー インコーポレーテッド | インテグリンレセプターアンタゴニスト |
EP0888344A1 (fr) | 1996-03-15 | 1999-01-07 | The Du Pont Merck Pharmaceutical Company | Inhibiteurs de l'integrine spirocycle |
DE59706273D1 (de) | 1996-03-20 | 2002-03-21 | Hoechst Ag | Inhibitoren der Knochenresorption und Vitronectinrezeptor-Antagonisten |
PT891325E (pt) | 1996-03-29 | 2002-07-31 | Searle & Co | Derivados do acido fenilpropanoico para-substituido como antagonistas de integrina |
DE69705300T2 (de) | 1996-03-29 | 2002-05-02 | Searle & Co | Cyclopropylalkansäurederivate |
EP0889876B1 (fr) | 1996-03-29 | 2001-07-25 | G.D. SEARLE & CO. | Derives meta-substitues du sulphonamide de phenylene |
ATE219764T1 (de) | 1996-03-29 | 2002-07-15 | Searle & Co | Zimtsäurederivate und deren verwendung als integrin-antagonisten |
DE69706407T2 (de) | 1996-03-29 | 2002-05-29 | Searle & Co | META-SUBSTITUIERTE PHENYLENDERIVATE UND IHRE VERWENDUNG ALS ALPHAvBETA3 INTERGRIN-ANTAGONISTEN ODER INHIBITOREN |
WO1997037655A1 (fr) | 1996-04-10 | 1997-10-16 | Merck & Co., Inc. | ANTAGONISTES DU RECEPTEUR αvβ3 |
DE19629816A1 (de) | 1996-07-24 | 1998-01-29 | Hoechst Ag | Neue Cycloalkyl-Derivate als Inhibitoren der Knochenresorption und Vitronectinrezeptor-Antagonisten |
DE19629817A1 (de) | 1996-07-24 | 1998-01-29 | Hoechst Ag | Neue Imino-Derivate als Inhibitoren der Knochenresorption und Vitronectinrezeptor-Antagonisten |
EP0934305A4 (fr) | 1996-08-29 | 2001-04-11 | Merck & Co Inc | Antagonistes de l'integrine |
WO1998018460A1 (fr) | 1996-10-30 | 1998-05-07 | Merck & Co., Inc. | Antagonistes de l'integrine |
EP0963370B1 (fr) | 1996-12-09 | 2003-03-19 | Eli Lilly And Company | Antagonistes de l'integrine |
DE19653646A1 (de) | 1996-12-20 | 1998-06-25 | Hoechst Ag | Substituierte Purinderivate, Verfahren zu deren Herstellung, sie enthaltende Mittel und deren Verwendung |
CO4920232A1 (es) | 1997-01-08 | 2000-05-29 | Smithkline Beecham Corp | Acidos aceticos dibenzo [a,d] cicloheptano con actividad antagonista del receptor de vitronectin |
JP2001509176A (ja) | 1997-01-17 | 2001-07-10 | メルク エンド カンパニー インコーポレーテッド | インテグリンアンタゴニスト |
DE19705450A1 (de) | 1997-02-13 | 1998-08-20 | Merck Patent Gmbh | Bicyclische aromatische Aminosäuren |
AU6780398A (en) | 1997-03-28 | 1998-10-22 | Du Pont Merck Pharmaceutical Company, The | Heterocyclic integrin inhibitor prodrugs |
WO1998046220A1 (fr) | 1997-04-14 | 1998-10-22 | Merck & Co., Inc. | Polytherapie pour la prevention et le traitement de l'osteoporose |
GB2327609A (en) | 1997-07-23 | 1999-02-03 | Merck & Co Inc | A method for eliciting an avß5 or dual avß3/avß5 antagonizing effect |
GB2327672A (en) | 1997-07-23 | 1999-02-03 | Merck & Co Inc | 4-(1,2,3,4-Tetrahydro-1,8-naphthyridin-7-yl)butanoyl-glycyl-3(S)-quinolin-3-yl-beta-alanine |
EP1000031A4 (fr) | 1997-07-25 | 2001-08-16 | Smithkline Beecham Corp | Antagonistes du recepteur de vitronectine |
AU2076299A (en) | 1998-01-30 | 1999-08-16 | Meiji Seika Kaisha Ltd. | Phenylpiperazine derivatives as integrin alphavbeta3 antagonists |
JP2003504301A (ja) * | 1998-04-01 | 2003-02-04 | ブリストル−マイヤーズ スクイブ ファーマ カンパニー | インテグリンアンタゴニスト |
ATE542797T1 (de) * | 1998-04-09 | 2012-02-15 | Meiji Seika Pharma Co Ltd | Aminopiperidinderivate als integrin alpha v beta 3 antagonisten |
-
2000
- 2000-08-02 US US10/048,914 patent/US6750219B1/en not_active Expired - Fee Related
- 2000-08-02 AU AU63169/00A patent/AU6316900A/en not_active Abandoned
- 2000-08-02 EP EP00949959A patent/EP1209152A4/fr not_active Withdrawn
- 2000-08-02 WO PCT/JP2000/005177 patent/WO2001010844A1/fr not_active Application Discontinuation
Non-Patent Citations (2)
Title |
---|
No further relevant documents disclosed * |
See also references of WO0110844A1 * |
Also Published As
Publication number | Publication date |
---|---|
EP1209152A1 (fr) | 2002-05-29 |
WO2001010844A1 (fr) | 2001-02-15 |
AU6316900A (en) | 2001-03-05 |
US6750219B1 (en) | 2004-06-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20020222 |
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AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE |
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AX | Request for extension of the european patent |
Free format text: AL;LT;LV;MK;RO;SI |
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A4 | Supplementary search report drawn up and despatched |
Effective date: 20030128 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION HAS BEEN WITHDRAWN |
|
18W | Application withdrawn |
Effective date: 20050728 |